Results for:
Species: CU Fusarium oxysporum oxysporum MSA 35

Compound Details

Synonymous names
Isolongipholene
Isolongifolene
trans-Isolongifolene
CQUAYTJDLQBXCQ-UHFFFAOYSA-N
AC1L2T2C
(-)-Isolongifoline
PL001072
AN-48692
AKOS015901700
FT-0694511
I14-14688
2,3A-ethanoindan, 3a,4,5,6-tetrahydro-1,1,4,4-tetramethyl-
2,2,7,7-TETRAMETHYLTRICYCLO[6.2.1.0(1),?]UNDEC-5-ENE
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (2S)-
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (2S-cis)-
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (2S,4aR)-(-)-
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (2S,4aR)-
IUPAC name
SMILESCC1(CCC=C2C13CCC(C3)C2(C)C)C
InchiInChI=1S/C15H24/c1-13(2)8-5-6-12-14(3,4)11-7-9-15(12,13)10-11/h6,11H,5,7-10H2,1-4H3
FormulaC15H24
PubChem ID102562
Molweight204.357
LogP4.11
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/aDickschat et al., 2005_3
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/aDickschat et al., 2005_3
BacteriaStreptomyces Sp. GWS-BW-H5.n/aDickschat et al., 2005_2
FungiCU Fusarium Oxysporum Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
FungiFusarium Oxysporum MSA 35long-distance antagonistic actionMinerdi et al. 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/an/a
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/an/a
BacteriaStreptomyces Sp. GWS-BW-H5.n/an/a
FungiCU Fusarium Oxysporum Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiFusarium Oxysporum MSA 35PDA/CMCAR/PDMS GCMSno


(1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene

Compound Details

Synonymous names
Caryophyllene
trans-Caryophyllene
NPNUFJAVOOONJE-GFUGXAQUSA-N
BETA-CARYOPHYLLENE
Beta-Caryophylene
trans-beta-caryophyllene
L-Caryophyllene
Caryophyllene B
AC1NQYK7
.beta.-Caryophyllen
.beta.-Caryophyllene
trans-.beta.-Caryophyllene
BHW853AU9H
(E)-Caryophyllene
.beta.-trans-Caryophyllene
AC1Q2A41
C15H24
UNII-BHW853AU9H
(E)-beta-caryophyllene
E-.beta.-caryophyllene
V0915
(E)-beta-caryophylene
NSC11906
CHEMBL445740
Caryophyllene, (E)
(-)-Caryophyllene
C09629
OR355343
(-)-trans-Caryophyllene
ST072181
DTXSID8024739
DR000334
DSSTox_CID_4739
CHEBI:10357
ZINC8234282
(-)-beta-caryophyllene
DSSTox_GSID_24739
(-)-trans-Caryophyllene, analytical standard
ZINC08234282
MFCD00075925
DSSTox_RID_77517
.beta.-(E)-Caryophyllene
W-109317
AKOS024283988
FT-0603049
LMPR0103120001
87-44-5
Tox21_301497
beta-Caryophyllene, >=80%, FCC, FG
(-)-(E)-Caryophyllene
CAS-87-44-5
NCGC00142620-01
NCGC00255159-01
.beta.-Caryophyllene, (-)
MolPort-001-793-250
(-)-trans-Caryophyllene, >=98.5% (sum of enantiomers, GC)
(1S,9R)-6,10,10-trimethyl-2-methylenebicyclo[7.2.0]undec-5-ene
trans-(1R,9S)-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene
trans-(1R,9S)-8-Methylene-4,11,11-trimethylbicyclo[7.2.0]undec-4-ene
(1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
(1R,4E,9S)-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene
(1R,4E,9S)-4,11,11-trimethyl-8-methylene-bicyclo[7.2.0]undec-4-ene
8-Methylene-4,11,11-(trimethyl)bicyclo(7.2.0)undec-4-ene, (1R,4E,9S)-
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (E)-(1R,9S)-(-)-
Bicyclo[7.2.0]undec-4-ene, 8-methylene-4,11,11-trimethyl-, (E)-(1R,9S)-(-)-
Bicyclo(7.2.0)undec-4-ene, 8-methylene-4,11,11-trimethyl-, (E)-(1R,9S)-(-)-
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, [1R-(1R*,4E,9S*)]-
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, [1R- (1R*,4E,9S*)]-
IUPAC name(1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
SMILESCC1=CCCC(=C)C2CC(C2CC1)(C)C
InchiInChI=1S/C15H24/c1-11-6-5-7-12(2)13-10-15(3,4)14(13)9-8-11/h6,13-14H,2,5,7-10H2,1,3-4H3/b11-6+/t13-,14-/m1/s1
FormulaC15H24
PubChem ID5281515
Molweight204.357
LogP4.52
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiPenicillium Clavigerumcompost Fischer et al. 2027
FungiCU Fusarium Oxysporum Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
FungiFusarium Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
FungiPaxillus Involutus MAJn/aMueller et al., 2013
FungiPaxillus Involutus NAUn/aMueller et al., 2013
FungiPhialophora Fastigiata ConantnanaSunesson et al., 1995
FungiTrichodema Viriden/aWheatley et al., 1997
FungiFusarium Oxysporum MSA 35long-distance antagonistic actionMinerdi et al. 2009
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPhoma Sp.n/aStrobel et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiPenicillium Clavigerumyest extract sucroseTenax/GC-MSno
FungiCU Fusarium Oxysporum Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiFusarium Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiPaxillus Involutus MAJMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus NAUMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPhialophora Fastigiata ConantDG18GC/MS
FungiTrichodema VirideMalt extractGC/MS
FungiFusarium Oxysporum MSA 35PDA/CMCAR/PDMS GCMSyes
FungiFomitopsis PinicolanaGC/MSNo
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPhoma Sp.n/aSolid phase microextraction (SPME)


4-ethenyl-4,9,9-trimethyl-6-methylidenebicyclo[5.2.0]nonane

Compound Details

Synonymous names
FITHEODIIYWPLM-UHFFFAOYSA-N
AC1LBUZB
CTK5J3403
4-ethenyl-4,9,9-trimethyl-6-methylidenebicyclo[5.2.0]nonane
4,8,8-Trimethyl-2-methylene-4-vinylbicyclo[5.2.0]nonane
4,8,8-Trimethyl-2-methylene-4-vinylbicyclo[5.2.0]nonane #
Bicyclo[5.2.0]nonane, 2-methylene-4,8,8-trimethyl-4-vinyl-
IUPAC name4-ethenyl-4,9,9-trimethyl-6-methylidenebicyclo[5.2.0]nonane
SMILESCC1(CC2C1CCC(CC2=C)(C)C=C)C
InchiInChI=1S/C15H24/c1-6-15(5)8-7-13-12(11(2)9-15)10-14(13,3)4/h6,12-13H,1-2,7-10H2,3-5H3
FormulaC15H24
PubChem ID564746
Molweight204.357
LogP4.48
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiCU Fusarium Oxysporum Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
FungiFusarium Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiCU Fusarium Oxysporum Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiFusarium Oxysporum MSA 35complete medium (CM)SPME/GC-MS


3,3-diethylhexane;4-methoxyphenol

Compound Details

Synonymous names
AC1LANTT
Butylated hydroxyanisol (bha)
3,3-diethylhexane; 4-methoxyphenol
IUPAC name3,3-diethylhexane;4-methoxyphenol
SMILESCCCC(CC)(CC)CC.COC1=CC=C(C=C1)O
InchiInChI=1S/C10H22.C7H8O2/c1-5-9-10(6-2,7-3)8-4;1-9-7-4-2-6(8)3-5-7/h5-9H2,1-4H3;2-5,8H,1H3
FormulaC17H30O2
PubChem ID517036
Molweight266.425
LogP4.61
Atoms49
Bonds48
H-bond Acceptor0
H-bond Donor0
Chemical Classificationethers alcohols benzenoids

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiCU Fusarium Oxysporum Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiCU Fusarium Oxysporum Oxysporum MSA 35complete medium (CM)SPME/GC-MS